Hamrick H J, Jennette J C, LaForce C F
J Allergy Clin Immunol. 1984 May;73(5 Pt 1):561-6. doi: 10.1016/0091-6749(84)90511-6.
A 14-year-old male adolescent is described with a 6-year history of active lymphadenopathy, skin rash, peripheral blood eosinophilia, and markedly elevated serum-IgE level. Complete histopathologic and immunologic evaluations established the diagnosis of Kimura's disease as first described in Japan. Because of its relative infrequency and varied features, this disorder can be difficult to diagnose when it is encountered in the United States.
一名14岁男性青少年，有6年的活动性淋巴结病、皮疹、外周血嗜酸性粒细胞增多及血清IgE水平显著升高病史。完整的组织病理学和免疫学评估确诊为日本首次描述的木村病。由于其相对罕见且特征多样，在美国遇到这种疾病时可能难以诊断。
